Language disorder with mild intellectual disability in a child affected by a novel mutation of SLC6A8 gene.
about
Inborn errors of creatine metabolism and epilepsy.Diagnostic methods and recommendations for the cerebral creatine deficiency syndromes.Neuropsychological profile and clinical effects of arginine treatment in children with creatine transport deficiency.Downregulation of the creatine transporter SLC6A8 by JAK2.Expression and distribution of creatine transporter and creatine kinase (brain isoform) in developing and mature rat cochlear tissues.Phenotype and genotype in 101 males with X-linked creatine transporter deficiency.
P2860
Language disorder with mild intellectual disability in a child affected by a novel mutation of SLC6A8 gene.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh-hant
name
Language disorder with mild in ...... novel mutation of SLC6A8 gene.
@en
Language disorder with mild in ...... novel mutation of SLC6A8 gene.
@nl
type
label
Language disorder with mild in ...... novel mutation of SLC6A8 gene.
@en
Language disorder with mild in ...... novel mutation of SLC6A8 gene.
@nl
prefLabel
Language disorder with mild in ...... novel mutation of SLC6A8 gene.
@en
Language disorder with mild in ...... novel mutation of SLC6A8 gene.
@nl
P2093
P50
P1476
Language disorder with mild in ...... novel mutation of SLC6A8 gene
@en
P2093
A Comparini
M Casarano
P304
P356
10.1016/J.YMGME.2010.11.005
P50
P577
2010-11-13T00:00:00Z